A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15320953



Internal ID5906352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92172749..92175313hg38UCSC Ensembl
Innerchr15:92172754..92175308hg38UCSC Ensembl
Outerchr15:92172744..92175318hg38UCSC Ensembl
chr15:92715979..92718543hg19UCSC Ensembl
Innerchr15:92715984..92718538hg19UCSC Ensembl
Outerchr15:92715974..92718548hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382565
hg192565
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637259
Supporting Variants
SamplesNA19320
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15320953
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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